Selby C P, Sancar A
Department of Biochemistry and Biophysics, University of North Carolina School of Medicine, Chapel Hill 27599.
Microbiol Rev. 1994 Sep;58(3):317-29. doi: 10.1128/mr.58.3.317-329.1994.
Mutation frequency decline is the rapid and irreversible decline in the suppressor mutation frequency of Escherichia coli cells if the cells are kept in nongrowth media immediately following the mutagenic treatment. The gene mfd, which is necessary for mutation frequency decline, encodes a protein of 130 kDa which couples transcription to excision repair by binding to RNA polymerase and to UvrA, which is the damage recognition subunit of the excision repair enzyme. Although current evidence suggests that transcription-repair coupling is the cause of the preferential repair of the transcribed strand of mRNA encoding genes as well as of suppressor tRNA genes, the decline occurs under stringent response conditions in which the tRNA genes are not efficiently transcribed. Thus, the mechanism of strand-specific repair is well understood, but some questions remain regarding the precise mechanism of mutation frequency decline.
突变频率下降是指,如果在诱变处理后立即将大肠杆菌细胞置于非生长培养基中,其抑制突变频率会迅速且不可逆地下降。基因mfd是突变频率下降所必需的,它编码一种130 kDa的蛋白质,该蛋白质通过与RNA聚合酶和UvrA结合,将转录与切除修复联系起来,UvrA是切除修复酶的损伤识别亚基。尽管目前的证据表明转录-修复偶联是编码基因的mRNA转录链以及抑制性tRNA基因优先修复的原因,但这种下降发生在严格反应条件下,此时tRNA基因不能有效转录。因此,链特异性修复的机制已得到充分理解,但关于突变频率下降的确切机制仍存在一些问题。